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Found 10 Stent trials

A listing of Stent medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

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99 years or below
All genders
Clinical data from this study will support the intended use of the Rapidlink device, a vascular prosthesis for replacement or bypass of diseased vessels in patients with aneurysmal or other vascular diseases. It is indicated for repair or replacement of aortic branch vessels during open aortic arch repair. Rapidlink simplifies …
18 years or above
All genders
Interventional
This study investigates the safety and effectiveness of an investigational endovascular graft system for treating aortic aneurysms. These aneurysms can involve one or more of the major visceral arteries, which supply blood to essential organs.Participants in the study will receive a combination of an investigational endovascular graft and other stent …
18 years or above
All genders
Interventional
This study investigates the Thor system for treating peripheral artery disease.The study evaluates the safety and effectiveness of the Thor system in treating calcified lesions in leg arteries.Who can participate: Adults aged 18 and older with peripheral artery disease and specific blockages in leg arteries may participate. Participants must be …
UPenn Stent-Graft Study
18 years - 99 years
All genders
This study will assess the feasibility and safety and to evaluate clinical outcomes of endovascular repair of complex aortic aneurysms (thoracoabdominal aortic aneurysms and aortic arch aneurysms or TAAA) in patients at high risk for open surgery in two study arms. Participants that choose to sign the informed consent and …
PK Papyrus Covered Coronary Stent System; H170004
99 years or below
All genders
The PK Papyrus Covered Coronary Stent System (PK Papyrus) received approval under a Humanitarian Device Exemption (HDE H170004) from the Food and Drug Administration on September 14, 2018 and is only indicated for treatment of acute perforations of native coronary arteries and coronary bypass grafts in vessels 2.5 to 5.0 …
TAMBE- Evaluation of the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis in the Treatment of Thoracoabdominal and Pararenal Aortic Aneurysms
18 years - 99 years
All genders
Normal 0 false false false EN-US JA X-NONE Patients with thoracoabdominal or pararenal aneurysm disease will be asked to take part in this research study This research study will look at treating thoracoabdominal or pararenal aneurysm disease with a new stent-graft design. The reason we are doing this research study …
JAGUAR- ObJective Analysis to GaUge EVAR Outcomes Through Randomization
21 years - 99 years
All genders
Phase 4
This post-approval study will collect safety, performance, effectiveness, and neck dilatation data on Alto Abdominal Stent Graft System for the endovascular treatment of infrarenal abdominal aortic aneurysms and evaluate real-world outcomes in comparison to commercially available comparator devices. Penn Medicine patients with the Alto Abdominal Stent Graft System, a device …
99 years or below
All genders
This is a prospective, multi-center, non-randomized, single arm, post-market study designed to evaluate the Thoraflex Hybrid device alone and in combination with the RelayPro NBS stent-graft in the treatment of aortic disease affecting the aortic arch and descending aorta with or without involvement of the ascending aorta.
18 years or above
All genders
Phase 1/2
Interventional
This study investigates the use of interstitial photodynamic therapy (I-PDT) following palliative radiotherapy in patients with inoperable malignant central airway obstruction. The purpose of this study is to test the safety and effectiveness of combining these treatments to improve tumor response and survival in patients whose airways are blocked by …
Product Surveillance Registry (PSR) Platform - Aortic, Peripheral & Venous (APV)
18 years - 100 years
All genders
Phase 4
This post-market registry serves as an ongoing source of product performance, patient safety, and clinical outcomes for a variety of different products. The research design allows products to be added once they are released on the market. Patients are enrolled and followed according to their care provider’s normal care routine.